Variant report

Variant	esv3333275
Chromosome Location	chr11:101418242-101420240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142554659	chr11:101418243-101418244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs60188740	chr11:101418245-101418246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12798282	chr11:101418257-101418258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558380380	chr11:101418262-101418263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4754767	chr11:101418263-101418264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543917972	chr11:101418274-101418275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563686689	chr11:101418290-101418291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73575787	chr11:101418291-101418292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541768717	chr11:101418305-101418306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4754768	chr11:101418322-101418323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs149312446	chr11:101418326-101418327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs118115878	chr11:101418327-101418328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4754769	chr11:101418353-101418354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs145581065	chr11:101418365-101418366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76286396	chr11:101418368-101418369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12791029	chr11:101418369-101418370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142541948	chr11:101418370-101418371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4754014	chr11:101418403-101418404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550156793	chr11:101418445-101418446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79725741	chr11:101418513-101418514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538011618	chr11:101418526-101418527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551210671	chr11:101418530-101418531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535313429	chr11:101418556-101418557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12793532	chr11:101418581-101418582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs4754770	chr11:101418615-101418616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537546147	chr11:101418622-101418623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558059734	chr11:101418647-101418648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373238419	chr11:101418670-101418671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557450998	chr11:101418709-101418710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574041476	chr11:101418733-101418734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543055020	chr11:101418737-101418738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185556798	chr11:101418819-101418820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572341109	chr11:101418825-101418826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4754771	chr11:101418845-101418846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563963478	chr11:101418938-101418939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7942189	chr11:101418944-101418945	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543121786	chr11:101418979-101418980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560363250	chr11:101418981-101418982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200983258	chr11:101418990-101418991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199523271	chr11:101418992-101418993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10633400	chr11:101418993-101418994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60683926	chr11:101419004-101419005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28612748	chr11:101419005-101419006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60991578	chr11:101419006-101419007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56777096	chr11:101419007-101419008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71303295	chr11:101419011-101419012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371108280	chr11:101419018-101419019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs58777127	chr11:101419020-101419021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547341337	chr11:101419038-101419039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113599106	chr11:101419067-101419068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101401200-101425800	Weak transcription	Ovary	ovary
2	chr11:101416400-101437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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